A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441997



Internal ID21099550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110123336..110154939hg38UCSC Ensembl
chr10:111883094..111914697hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3831604
hg1931604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195918
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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